TRABAJO STUDY START UP REGULATORY

As study start up manager, you will lead a team of study start up associates across europe  (size of team up to 18 fte) within our study start up team...

Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations... provide specialist regulatory and technical scientific...

As a study start up associate at icon, you’ll work within a large-scale, fast-paced environment assisting the study start up team lead in the development of the...

As study start up manager dedicated to site contracts, you will lead a team of study start up associates across europe  (size of team up to fte) within our study...

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team...

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team,...

study start up associate ii as a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

study start up associate iias a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

As a clinical study start up lead - senior manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered...

Perform start up and site activation activities according to applicable regulations, sops and work instructions... prepare site regulatory documents, reviewing for...

up to date on latest regulatory requirements in europe and share potential impact to the involved parties... sure that the regulatory database is up to date for...

Support the study team in the implementation of audits and regulatory inspections... support risk management and quality efforts to ensure study compliance...

• experience in all phases of a clinical study lifecycle... • extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities...

updated knowledge of national/international regulations relative to clinical trial start up procedures... description: we have an open position for a lead regulatory...

Manages study supplies (isf, etc), drug supplies and drug accountability at study site... prepares study drug for destruction, if applicable... ensures timely collection/uploading...

(inter)national coordinating investigators, steering/executive committee) during study design and delivery   manage study finance:    develop and maintain the overall...